Karyopharm KPT-IST-391 (Relapsed/Refractory Multiple Myeloma) - Clinical Trial

What is the Purpose of this Study?

We are doing this study to find out if an experimental combination of drugs (selinexor, ruxolitinib, and methylprednisolone) is a safe and effective option for treating multiple myeloma that has come back after treatment or is not responding to treatment.

What is the Condition Being Studied?

Relapsed/Refractory Multiple Myeloma

Who Can Participate in the Study?

Adults ages 18+ who:

  • Are diagnosed with multiple myeloma that has 1 of the following features: clonal bone marrow plasma cells >10% or biopsy-proven bony or extramedullary plasmacytoma
  • Did not have an adequate response to treatment that included the following drugs: anti-CD38 antibody, immunomodulatory agent, proteasome inhibitor

For more information, contact the study team at quinna.marshburn@duke.edu.

Age Group
Adults

What is Involved?

Everyone who takes part in this study will receive the study drug regimen. No placebo is used in this study.

If you choose to join, you will:

  • Take selinexor once per week
  • Take ruxolitinib twice per day
  • Take methylprednisolone every other day

Your progress will be assessed at the end of each 28-day period of taking the study regimen. These 28-day periods are called "cycles." The number of cycles you do in this study will depend on how you respond to the study drug regimen.

Study Details

Full Title
A phase I trial of selinexor, ruxolitinib and methylprednisolone for patients with relapsed/refractory multiple myeloma
Principal Investigator
Hematologic Oncologist
Protocol Number
IRB: PRO00117038
NCT: NCT06225310
Phase
Phase I
ClinicalTrials.gov
Enrollment Status
Open for Enrollment